Long noncoding RNA ZFAS1 suppresses osteogenic differentiation of bone marrow-derived mesenchymal stem cells by upregulating miR-499-EPHA5 axis

被引:18
|
作者
Wu, Jinhui [1 ]
Lin, Tao [1 ]
Gao, Yang [2 ]
Li, Xiaoming [3 ]
Yang, Chen [1 ]
Zhang, Ke [1 ]
Wang, Ce [1 ]
Zhou, Xuhui [1 ]
机构
[1] Second Mil Med Univ, Changzheng Hosp, Dept Orthoped, 415 Fengyang Rd, Shanghai 200003, Peoples R China
[2] Chinese Peoples Liberat Army Gen Hosp, Med Sch Chinese PLA, Dept Orthoped, Natl Clin Res Ctr Orthopaed, Beijing 100853, Peoples R China
[3] 98 Hosp PLA, Dept Orthopaed, Huzhou 313000, Peoples R China
关键词
Osteoporosis; Bone marrow-derived mesenchymal stem cells; ZFAS1-miR-499-EPHA5; Osteogenic differentiation; Adipogenic differentiation; OSTEOBLAST;
D O I
10.1016/j.mce.2021.111490
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Emerging evidence suggests that the shift between osteogenic and adipogenic differentiation of bone marrowderived mesenchymal stem cells (BMSCs) determines bone mass. Our study was aimed at testing whether a long noncoding RNA called zinc finger antisense 1 (ZFAS1) participates in the differentiation commitment of BMSCs during osteoporosis. We found that ZFAS1 expression was downregulated during osteogenic differentiation and upregulated during adipogenic differentiation. ZFAS1 knockdown facilitated osteogenic differentiation and suppressed adipogenic differentiation. Furthermore, ZFAS1 knockdown suppressed cell senescence and promoted autophagy. Ovariectomized mice injected with a ZFAS1 knockdown construct showed increased bone mass. Mechanismly, ZFAS1 affected the osteogenic and adipogenic differentiation of BMSCs through sponging miR-499 thereby upregulating ephrin type-A receptor 5 (EPHA5). Taken together, our results revealed that the ZFAS1-miR-499-EPHA5 axis may be important for the osteoporosis-related switch between the osteogenesis and adipogenesis of BMSCs, indicating that ZFAS1 represents a plausible therapeutic target for reversing osteoporotic bone loss.
引用
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页数:9
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